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Arylsulfatase B 抗体 (C-Term)

This anti-Arylsulfatase B antibody is a 兔 多克隆 antibody detecting Arylsulfatase B in WB, ELISA, IHC (p) 和 IF. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN6991898
发货至: 中国

Quick Overview for Arylsulfatase B 抗体 (C-Term) (ABIN6991898)

抗原

See all Arylsulfatase B (ARSB) 抗体
Arylsulfatase B (ARSB)

适用

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人, 小鼠, 大鼠

宿主

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克隆类型

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多克隆

标记

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This Arylsulfatase B antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)
  • 抗原表位

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    AA 460-510, C-Term

    特异性

    ARSB antibody is human, mouse and rat reactive. At least two isoforms of ARSB are known to exist, this antibody only recognizes the longest isoform.

    纯化方法

    ARSB Antibody is affinity chromatography purified via peptide column.

    免疫原

    ARSB antibody was raised against a 16 amino acid peptide near the carboxy terminus of human ARSB. The immunogen is located within amino acids 460 - 510 of ARSB .

    亚型

    IgG
  • 应用备注

    ARSB antibody can be used for detection of ARSB by Western blot at 1 - 2 μ,g/mL.

    Antibody validated: Western Blot in mouse samples, Immunohistochemistry in human samples and Immunofluorescence in human samples. All other applications and species not yet tested.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    ARSB Antibody is supplied in PBS containing 0.02 % sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C,4 °C

    储存方法

    ARSB antibody can be stored at 4°C for three months and -20°C, stable for up to one year.
  • 抗原

    Arylsulfatase B (ARSB)

    别名

    ARSB

    背景

    Aryl sulfatase B (ARSB) forms a homodimer that hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate (1). ARSB localizes to the lysozyme as well as to the extracellular matrix (2). Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B (3), and can be treated with exogenous ARSB (4).

    分子量

    Predicted: 59 kDa

    Observed: 57kDa

    基因ID

    411

    NCBI登录号

    NP_000037

    UniProt

    P15848

    途径

    Glycosaminoglycan Metabolic Process
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